United States· US:69729-223_56ab1a6f-9733-820a-e063-6294a90aaa97
Pentrexcilina Daytime
A medicinal product containing phenylephrine hydrochloride; chlorpheniramine maleate; acetaminophen, registered in United States by OPMX LLC.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- PHENYLEPHRINE HYDROCHLORIDE; CHLORPHENIRAMINE MALEATE; ACETAMINOPHEN
- Manufacturer
- OPMX LLC
- Country
- United States (US)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 5
- ndc1169729-223-02
- ndc1169729-223-06
- ndc1169729-223-37
- ndc1169729-223-38
- ndc1169729-223-50
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Phenylephrine hydrochloride; chlorpheniramine maleate; acetaminophen in 3 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SpainABACAT GRANULADO PARA SOLUCIÓN ORAL.Tarbis Farma S.L.
- PolandFlucontrol HotAflofarm Farmacja Polska Sp. z o.o.
- CanadaBENYLIN EXTRA STRENGTH COLD & SINUS NIGHTMCNEIL CONSUMER HEALTHCARE DIVISION OF JOHNSON & JOHNSON INC
Authorised across Europe · EMA
The same active substance is authorised in 5 EEA countries. Names it is sold under:
- Bulgaria · Тайлолфен Хот
- Spain · Abacat, Anticatarral Edigen
- Malta · Flucontrol Max
- Poland · Flucontrol Hot, Flucontrol Max
- Portugal · Gripalgin
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/930bafb9-0078-461f-aedc-b20796596449 GET /v1/drugs/930bafb9-0078-461f-aedc-b20796596449?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"route": "ORAL",
"source": "ndc",
"strength": "10; 4; 500",
"substance": "PHENYLEPHRINE HYDROCHLORIDE; CHLORPHENIRAMINE MALEATE; ACETAMINOPHEN",
"productndc": "69729-223",
"dosage_form": "TABLET",
"dea_schedule": null,
"strength_unit": "mg/1; mg/1; mg/1",
"application_number": "M012",
"marketing_category": "OTC MONOGRAPH DRUG"
}See everything about phenylephrine hydrochloride; chlorpheniramine maleate; acetaminophen.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.